# (Sr.) Site Activation Specialist

**Company**: IQVIA
**Location**: Frankfurt, Hesse
**Work arrangement**: remote
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Frankfurt-Hesse-Germany/XMLNAME--Sr--Site-Activation-Specialist--m-w-d-_R1572145?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_4aabb566-a48

## Description

IQVIA currently offers the exciting opportunity for a (Sr.) Site Activation Specialist to work in the Country Site Activation Department home-based within Germany.

In this role you will perform tasks at a country level associated with clinical research site activation activities in accordance with applicable local and/or international regulations, standard operating procedures, project requirements and contractual/budgetary guidelines.

**Your responsibilities might include:**

- Serve as Single Point of Contact in assigned studies for investigative sites, RSU Team Lead, Clinical Operations, Feasibility, Site Identification, Project Management and the client.

- Ensure adherence to standard operating procedures (SOPs), work instructions, quality of designated deliverables and to project timelines.

- Perform Regulatory, Start-up and Maintenance activities according to applicable regulations, SOPs and work instructions.

- Review, prepare and negotiate site contracts and budgets with sites. Prepare site regulatory documents, reviewing for completeness and accuracy. Perform quality control of documents provided by sites.

- Complete and submit approval request documents to Local Regulatory and Ethical Committees. Ensure regulatory documents and approvals are granted, IP Release authorized and specific project deliverables are completed.

- Review, track and follow up the progress, the approval and execution of documents, including contracts, regulatory, ethics ICF and IP Release documents, in line with project timelines.

- Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.

- Review, establish and agree on project planning and project timelines. Ensure overall project efficiency and adherence to project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.

- Review and provide feedback to management on site performance metrics.

**Qualifications:**

- University Degree in life science or other scientific discipline or apprenticeship in health care or as legal secretary / paralegal.

- Clinical research experience, preferable in study start-up, alternatively an equivalent combination of education, training and experience.

- Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

- Fluent language skills in German (on at least C1 level) and a good command of English.

- Strong written and verbal communication skills.

- Attention to detail and ability to work on multiple tasks and prioritize.

**What you can expect:**

- Supportive leaders, mentors and teams.

- Resources that promote your career growth.

- Dynamic work environments that expose you to new experiences.

- Flexible working schedule and home-office.

- Competitive salary, bonus system, pension and more.

## Skills

### Required
- Good Clinical Practice (GCP)
- International Conference on Harmonization (ICH)
- German
- English
- life science
- clinical research

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Frankfurt-Hesse-Germany/XMLNAME--Sr--Site-Activation-Specialist--m-w-d-_R1572145?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)